Fig. 1From: Targeted gene correction and functional recovery in achondroplasia patient-derived iPSCsIdentification, isolation and culture of somatic cells from ACH patients. a DNA sequences of the three ACH patients showed that these disorders were all caused by heterozygous mutations of Gly380Arg in the FGFR3. b, c SFs from the girl and the boy. d, e UC colonies from the girl and the boy showed epithelial cell morphology. f, g AD-MSCs from the adult male exhibited a typical fibroblast-like morphology. Bar in all panels: 10 μmBack to article page